Canonical Allele Identifier: CA1980172535

Gene: AIP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67490589_67490594delinsCCTCTA , CM000673.2:g.67490589_67490594delinsCCTCTA	GRCh38
NC_000011.9:g.67258060_67258065delinsCCTCTA , CM000673.1:g.67258060_67258065delinsCCTCTA	GRCh37
NC_000011.8:g.67014636_67014641delinsCCTCTA	NCBI36
NG_008969.1:g.12556_12561delinsCCTCTA , LRG_460:g.12556_12561delinsCCTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525341.2:c.896_901delinsCCTCTA
ENST00000528641.7:c.598+132_598+137delinsCCTCTA	ENSP00000434982.3:n.598+132_598+137delinsCCTCTA
ENST00000529797.2:n.1431_1436delinsCCTCTA
ENST00000682324.1:c.469-408_469-403delinsCCTCTA	ENSP00000508017.1:n.469-408_469-403delinsCCTCTA
ENST00000682659.1:c.418+132_418+137delinsCCTCTA	ENSP00000507351.1:n.418+132_418+137delinsCCTCTA
ENST00000682699.1:c.787+132_787+137delinsCCTCTA	ENSP00000507935.1:n.787+132_787+137delinsCCTCTA
ENST00000683237.1:c.779+140_779+145delinsCCTCTA	ENSP00000507343.1:n.779+140_779+145delinsCCTCTA
ENST00000683856.1:c.610+132_610+137delinsCCTCTA	ENSP00000507979.1:n.610+132_610+137delinsCCTCTA
ENST00000684006.1:c.787+132_787+137delinsCCTCTA	ENSP00000507269.1:n.787+132_787+137delinsCCTCTA
ENST00000684657.1:c.607+132_607+137delinsCCTCTA	ENSP00000507961.1:n.607+132_607+137delinsCCTCTA
ENST00000279146.8:c.787+132_787+137delinsCCTCTA MANE Select	ENSP00000279146.3:n.787+132_787+137delinsCCTCTA
ENST00000279146.7:c.787+132_787+137delinsCCTCTA	ENSP00000279146.3:n.787+132_787+137delinsCCTCTA
ENST00000525341.1:c.571_576delinsCCTCTA	ENSP00000476993.1:n.571_576delinsCCTCTA
ENST00000528641.6:c.598+132_598+137delinsCCTCTA	ENSP00000434982.2:n.598+132_598+137delinsCCTCTA
NM_001302959.1:c.610+132_610+137delinsCCTCTA	NP_001289888.1:n.610+132_610+137delinsCCTCTA
NM_001302960.1:c.779+140_779+145delinsCCTCTA	NP_001289889.1:n.779+140_779+145delinsCCTCTA
NM_003977.3:c.787+132_787+137delinsCCTCTA	NP_003968.3:n.787+132_787+137delinsCCTCTA
XM_024448761.1:c.787+132_787+137delinsCCTCTA	XP_024304529.1:n.787+132_787+137delinsCCTCTA
NM_003977.4:c.787+132_787+137delinsCCTCTA MANE Select	NP_003968.3:n.787+132_787+137delinsCCTCTA
NM_001302960.2:c.779+140_779+145delinsCCTCTA	NP_001289889.1:n.779+140_779+145delinsCCTCTA
NM_001302959.2:c.610+132_610+137delinsCCTCTA	NP_001289888.1:n.610+132_610+137delinsCCTCTA